Premium
Molecular‐Level Design of Pyrrhotite Electrocatalyst Decorated Hierarchical Porous Carbon Spheres as Nanoreactors for Lithium–Sulfur Batteries
Author(s) -
Boyjoo Yash,
Shi Haodong,
Olsson Emilia,
Cai Qiong,
Wu ZhongShuai,
Liu Jian,
Lu Gao Qing Max
Publication year - 2020
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.202000651
Subject(s) - nanoreactor , materials science , electrocatalyst , pyrrhotite , chemical engineering , carbon fibers , lithium (medication) , sulfur , nanoparticle , porosity , lithium–sulfur battery , nanotechnology , electrode , electrochemistry , composite number , chemistry , composite material , metallurgy , endocrinology , medicine , engineering
Lithium–sulfur batteries (LSBs) are a class of new‐generation rechargeable high‐energy‐density batteries. However, the persisting issue of lithium polysulfides (LiPs) dissolution and the shuttling effect that impedes the efficiency of LSBs are challenging to resolve. Herein a general synthesis of highly dispersed pyrrhotite Fe 1− x S nanoparticles embedded in hierarchically porous nitrogen‐doped carbon spheres (Fe 1− x S‐NC) is proposed. Fe 1− x S‐NC has a high specific surface area (627 m 2 g −1 ), large pore volume (0.41 cm 3 g −1 ), and enhanced adsorption and electrocatalytic transition toward LiPs. Furthermore, in situ generated large mesoporous pores within carbon spheres can accommodate high sulfur loading of up to 75%, and sustain volume variations during charge/discharge cycles as well as improve ionic/mass transfer. The exceptional adsorption properties of Fe 1− x S‐NC for LiPs are predicted theoretically and confirmed experimentally. Subsequently, the electrocatalytic activity of Fe 1− x S‐NC is thoroughly verified. The results confirm Fe 1− x S‐NC is a highly efficient nanoreactor for sulfur loading. Consequently, the Fe 1− x S‐NC nanoreactor performs extremely well as a cathodic material for LSBs, exhibiting a high initial capacity of 1070 mAh g −1 with nearly no capacity loss after 200 cycles at 0.5 C. Furthermore, the resulting LSBs display remarkably enhanced rate capability and cyclability even at a high sulfur loading of 8.14 mg cm −2 .